Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs11555978
- Species
- Homo sapiens
- Symbol
- rs11555978
- Category
- Variant
- Variant type
- SNP
- Overlaps
- POLDIP2
- Location
- 17:28357342
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000017.11:g.28357342G>A
- HGVS.c name
- ENSEMBL:ENST00000540200.6:c.107C>T
- ENSEMBL:ENST00000618887.2:c.107C>T
- HGVS.p name
- ENSP00000475924:p.Ala36Val
- ENSP00000477665:p.Ala36Val
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:28346633...28357527 (10.89 kb)
- Assembly version
- Not Available
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